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2475 Improvement of Iron Overload Parameters in Patients with Transfusion-Dependent β-Thalassemia Treated with Luspatercept: Data from the Phase 3b Long-Term Rollover Study Following the BELIEVE Trial

Program: Oral and Poster Abstracts
Session: 112. Thalassemia and Globin Gene Regulation: Poster II
Hematology Disease Topics & Pathways:
Research, Clinical trials, Iron Overload, Clinical Research, Thalassemia, Hemoglobinopathies, Diseases, Metabolic Disorders
Sunday, December 8, 2024, 6:00 PM-8:00 PM

John B. Porter1*, Maria Domenica Cappellini, MD2, Kevin H.M. Kuo, MD, MSc, FRCPC3,4, Maria Dimopoulou5*, Marta Reverte6*, Loyse Felber Medlin6*, Shweta Sharma7*, Kefeng Wang8*, Jennie Zhang8* and Ali T. Taher, MD, FRCP9

1University College London, University College London Hospitals, London, United Kingdom
2Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, SC Medicina ad Indirizzo Metabolico, Milan, Italy
3Division of Medical Oncology and Hematology, Department of Medicine, University Health Network, Toronto, ON, Canada
4Division of Hematology, Department of Medicine, University of Toronto, Toronto, ON, Canada
5Thalassemia Unit Centre of Expertise in Hemoglobinopathies, Laiko General Hospital of Athens, Athens, Greece
6Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland
7Bristol Myers Squibb, New Delhi, India
8Bristol Myers Squibb, Princeton, NJ
9Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon

Introduction: Patients (pts) with transfusion-dependent (TD) β-thalassemia require lifelong red blood cell (RBC) transfusions, which can contribute to iron overload and increased morbidity and mortality. In the phase 3 BELIEVE trial (NCT02604433), treatment with luspatercept reduced transfusion burden (TB) with a manageable safety profile. At the end of the BELIEVE trial, pts receiving luspatercept were eligible for the open-label, phase 3b long-term follow-up (LTFU) study (NCT04064060). The aim of this analysis was to evaluate the effect of long-term luspatercept treatment on iron parameters in pts who entered the LTFU study from the BELIEVE trial.

Methods: This analysis included pts randomized to luspatercept during the BELIEVE trial (luspatercept group) and pts randomized to placebo who crossed over to receive luspatercept after unblinding (crossover group). For crossover pts, treatment timing was defined from initiation of luspatercept treatment. Serum ferritin (SF) levels, liver iron concentration (LIC) by MRI (derived from T2*, R2*, or R2 method), and changes in iron chelation therapy (ICT) use were evaluated per 48-wk intervals alongside changes in RBC TB. Mean changes from baseline (BL) were calculated using values from evaluable pts. BL values for SF and ICT use were calculated for the 12 wk prior to first dose and at the last assessment on/before the first dose for LIC; BL values for crossover pts were prior to starting placebo. The data cutoff was Jan 28, 2024.

Results: Median (range) treatment duration over the combined BELIEVE and LTFU studies was 229.1 wk (1.7–388.6) for the luspatercept group and 225.9 wk (6.1–286.6) for the crossover group. Median (range) follow-up was 303.3 wk (1.7–392.0) and 268.1 wk (11.1–286.6), respectively. At data cutoff, 111 pts had ongoing treatment: 72/224 (32.1%) in the luspatercept group and 39/92 (42.4%) in the crossover group. Concomitant ICT was received by > 98% of pts, with 72% (n = 161) in the luspatercept group and 74% (n = 68) in the crossover group receiving deferasirox.

In the luspatercept group, mean change from BL in SF ranged from −247.2 μg/L to −541.3 μg/L during wk 48–384. Overall mean change from BL in SF at efficacy cutoff was −374.1 μg/L (standard deviation [SD] 1209.4) from a median BL of 1416.0 μg/L (range, 88.0–6400.0). In the crossover group, SF levels began to decrease from wk 144; however, overall SF was similar to BL: overall mean change from BL at efficacy cutoff was 21.2 μg/L (SD 1128.8) from a median BL of 1241.0 μg/L (range, 136.0–6400.0). In the luspatercept group, 42.6% of pts with BL SF ≥ 1000 μg/L shifted to SF < 1000 μg/L by efficacy cutoff. Similarly, 34.9% of pts in the crossover group shifted to < 1000 μg/L versus BL.

Median (range) LIC at BL was 5.9 mg/g dry weight (dw) (0.8–42.0) in the luspatercept group and 4.6 mg/g dw (0.2–43.0) in the crossover group. LIC values remained near BL up to wk 96 in the luspatercept group, after which only small reductions from BL were observed (mean change ranged from −3.1 to 0.2 mg/g dw during wk 96–336). In the crossover group, LIC values were similar to BL; mean change from BL during wk 96–288 ranged from −0.2 to 1.5 mg/g dw.

ICT use decreased from BL in the luspatercept group, particularly for deferasirox, for which the mean change from BL in daily dose ranged from −103.4 mg to −192.4 mg during wk 144–240. In the crossover group, mean daily deferasirox dose decreased through wk 288, with the highest reductions from BL seen at wk 48 (−252.5 mg), wk 96 (−204.9 mg), and wk 240 (−198.0 mg).

A decrease in RBC TB from BL was maintained in both the luspatercept (through wk 336) and crossover (through wk 240) groups. At each interval, the mean reduction in the number of RBC units transfused ranged from 4.8 to 7.8 units/48 wk and 5.1 to 6.9 units/48 wk for the luspatercept and crossover groups, respectively, representing a mean reduction from BL of ~20% (mean reductions ranging from 17.4% to 26.8% and 17.0% to 25.0%, respectively).

Conclusions: Long-term treatment with luspatercept (median duration > 4 y) resulted in decreased SF maintained below BL levels. Furthermore, LIC remained stable despite lower daily doses of deferasirox. The stabilization or improvement in iron parameters is likely attributable to the sustained reduction in RBC TB with luspatercept treatment. This analysis supports the overall long-term benefit of luspatercept in pts with TD β‑thalassemia, potentially alleviating iron overload and preventing future complications.

Disclosures: Porter: Silence therapeutics: Consultancy, Research Funding; bluebird bio: Consultancy; Bristol Myers Squibb (Celgene): Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Agios Pharmaceuticals, Inc.: Consultancy; Vifor: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees; Agios: Honoraria, Membership on an entity's Board of Directors or advisory committees. Cappellini: Bristol Myers Squibb (Celgene): Membership on an entity's Board of Directors or advisory committees; Sanofi-Genzyme: Membership on an entity's Board of Directors or advisory committees; Silence: Membership on an entity's Board of Directors or advisory committees; Vifor: Membership on an entity's Board of Directors or advisory committees; Pfizer: Membership on an entity's Board of Directors or advisory committees; Vertex Pharmaceuticals: Membership on an entity's Board of Directors or advisory committees; Agios Pharmaceuticals, Inc.: Membership on an entity's Board of Directors or advisory committees; Pharmacosmos: Membership on an entity's Board of Directors or advisory committees; Novo Nordisk: Membership on an entity's Board of Directors or advisory committees. Kuo: Agios Pharmaceuticals, Inc.: Consultancy, Honoraria, Membership on an entity's Board of Directors or advisory committees, Research Funding; Vertex Pharmaceuticals: Consultancy, Honoraria; Pfizer: Consultancy, Research Funding; Sangamo: Membership on an entity's Board of Directors or advisory committees; Forma Therapeutics: Consultancy; Bristol Myers Squibb: Consultancy, Honoraria; Biossil: Consultancy; Novo Nordisk: Consultancy; Alexion Pharmaceuticals: Consultancy, Honoraria. Dimopoulou: Bristol Myers Squibb: Consultancy, Honoraria, Research Funding; Pfizer: Consultancy, Honoraria; Novo Nordisk: Consultancy; Celgene: Research Funding; Agios: Research Funding; Pharmacosmos: Research Funding; Theravia: Research Funding. Reverte: Bristol Myers Squibb: Current Employment, Current equity holder in publicly-traded company. Felber Medlin: Bristol Myers Squibb: Current Employment, Current equity holder in publicly-traded company. Sharma: Syneos Health: Current Employment, Other: FSP consultant for BMS. Wang: Bristol Myers Squibb: Current Employment. Zhang: Bristol Myers Squibb: Current Employment, Current equity holder in publicly-traded company. Taher: Vifor: Consultancy, Research Funding; Pharmacosmos: Consultancy, Research Funding; Novo Nordisk: Consultancy; Bristol Myers Squibb (Celgene): Consultancy, Research Funding; Agios Pharmaceuticals, Inc.: Consultancy, Research Funding.

*signifies non-member of ASH